Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J W Callahan

Showing results (41-50 of 72) with videos related to

Pageof 8
Sort By:
Canadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire|June 1, 1984
Human placental beta-galactosidase: structural and immunological observationsC S Jones, D Mahuran, J A Lowden, et al.
Biochemical Medicine|June 1, 1973
Alpha-N-acetylgalactosaminidase: isolation, properties and distribution of the human enzymeJ W Callahan, E L Lassila, W Den Tandt, et al.
Biochimica Et Biophysica Acta|November 2, 1978
Concanavalin A promotes the uptake of lysosomal hydrolases by human fibroblastsR L Juliano, M R Moore, J W Callahan, et al.
The Biochemical Journal|February 1, 1996
Early proteolytic cleavage with loss of a C-terminal fragment underlies altered processing of the beta-galactosidase precursor in galactosialidosisY Okamura-Oho, S Zhang, W Hilson, et al.
Experimental Cell Research|April 1, 1979
Lectin-mediated uptake of lysosomal hydrolases by genetically deficient human fibroblastsR L Juliano, M R Moore, J W Callahan, et al.
The Biochemical Journal|August 1, 1992
Characteristics of the beta-galactosidase-carboxypeptidase complex in GM1-gangliosidosis and beta-galactosialidosis fibroblastsR M D'Agrosa, M Hubbes, S Zhang, et al.
Archives of Neurology|July 1, 1972
Niemann-Pick disease (Crocker's group A). Late onset and pigmentary degeneration resembling Hallervorden-Spatz syndromeJ J Martin, M Philippart, J Van Hauwaert, et al.
Clinical Biochemistry|December 1, 1990
First trimester prenatal diagnosis of Tay-Sachs disease using the sulfated synthetic substrate for hexosaminidase AJ W Callahan, A Archibald, M A Skomorowski, et al.
The Biochemical Journal|February 1, 1983
Studies on the structure of sphingomyelinase. Amino acid composition and heterogeneity on isoelectric focusingC S Jones, P Shankaran, D J Davidson, et al.
The Journal of Pediatrics|April 1, 1986
Ocular involvement in Niemann-Pick disease type BM H Lipson, J O'Donnell, J W Callahan, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Canadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire|June 1, 1984
Human placental beta-galactosidase: structural and immunological observationsC S Jones, D Mahuran, J A Lowden, et al.
Biochemical Medicine|June 1, 1973
Alpha-N-acetylgalactosaminidase: isolation, properties and distribution of the human enzymeJ W Callahan, E L Lassila, W Den Tandt, et al.
Biochimica Et Biophysica Acta|November 2, 1978
Concanavalin A promotes the uptake of lysosomal hydrolases by human fibroblastsR L Juliano, M R Moore, J W Callahan, et al.
The Biochemical Journal|February 1, 1996
Early proteolytic cleavage with loss of a C-terminal fragment underlies altered processing of the beta-galactosidase precursor in galactosialidosisY Okamura-Oho, S Zhang, W Hilson, et al.
Experimental Cell Research|April 1, 1979
Lectin-mediated uptake of lysosomal hydrolases by genetically deficient human fibroblastsR L Juliano, M R Moore, J W Callahan, et al.
The Biochemical Journal|August 1, 1992
Characteristics of the beta-galactosidase-carboxypeptidase complex in GM1-gangliosidosis and beta-galactosialidosis fibroblastsR M D'Agrosa, M Hubbes, S Zhang, et al.
Archives of Neurology|July 1, 1972
Niemann-Pick disease (Crocker's group A). Late onset and pigmentary degeneration resembling Hallervorden-Spatz syndromeJ J Martin, M Philippart, J Van Hauwaert, et al.
Clinical Biochemistry|December 1, 1990
First trimester prenatal diagnosis of Tay-Sachs disease using the sulfated synthetic substrate for hexosaminidase AJ W Callahan, A Archibald, M A Skomorowski, et al.
The Biochemical Journal|February 1, 1983
Studies on the structure of sphingomyelinase. Amino acid composition and heterogeneity on isoelectric focusingC S Jones, P Shankaran, D J Davidson, et al.
The Journal of Pediatrics|April 1, 1986
Ocular involvement in Niemann-Pick disease type BM H Lipson, J O'Donnell, J W Callahan, et al.
Pageof 8